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Overview In this role you will monitor clinical studies across investigative sites, ensuring adherence to protocol, SOPs, ICH-GCP, and applicable regulations. You will coordinate study setup and monitoring activities, including investigator...Read More>>.

Overview As a Senior Clinical Research Associate, you will help build and shape Quotient Sciences' clinical monitoring function across early-phase trials. You will partner with Clinical Operations, Quality Assurance and study teams to uphol...Read More>>.

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Overview As a CRA at Parexel, you will go beyond traditional monitoring to safeguard patient wellbeing and ensure study success across UK sites. You’ll manage site relationships, oversee quality from site identification to close-out, and...Read More>>.

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Overview In this role you support the execution of interventional studies as a Clinical Research Associate within IQVIA's sponsor-dedicated team. You will conduct on-site monitoring and ensure compliance with GCP/ICH while collaborating wit...Read More>>.

Overview As a CRA II in the UK, you monitor and manage clinical site performance to ensure regulatory and protocol compliance. You will work within the Clinical Solutions group, collaborating with cross-functional teams to support data qual...Read More>>.

Overview In this Senior CRA role, you will oversee site management, monitoring, and close-out for assigned investigative sites to safeguard patient safety and ensure high-quality study execution. You’ll manage operational activities from...Read More>>.

Overview In this Senior CRA role, you will lead and execute site-centric activities to deliver high-quality clinical studies for a key sponsor. You will collaborate with local study teams to ensure patient safety, regulatory compliance, and...Read More>>.

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Get AI-powered advice on this job and more exclusive features.Direct message the job poster from EPM ScientificConsultant at EPM Scientific | Permanent SolutionsWe're currently partnering with a leading international pharmac...Read More>>.

Join to apply for the Senior Clinical Research Associate role at TFS HealthScience3 weeks ago Be among the first 25 applicantsJoin to apply for the Senior Clinical Research Associate...Read More>>.

IQVIA LLC is seeking a site-based Clinical Research Associate to manage monitoring activities and ensure regulatory compliance across trials in Leeds. You will track submissions, site recruitment, data queries and documentation, while maintaining...Read More>>.

IQVIA is seeking an experienced Clinical Monitoring professional to oversee site visits and ensure protocol adherence across multiple sites in the United States. You will drive recruitment planning and manage regulatory submissions while maintaini...Read More>>.

Durham, North Carolina, United States of America Aurora, Illinois, United States San Fernando, California, United States Clinton, Missouri, United States Mansfield, Ohio, United States Santa Cruz, California, Uni...Read More>>.

Tigermed is seeking an experienced CRA to oversee site management, training, documentation, safety reporting, finance, and tool maintenance across multiple studies. The role requires in-depth knowledge of ICH-GCP and clinical trial operations, wit...Read More>>.

Job Title: Research Associate in the Digital Validation of Engineered Porous Structures, LoughboroughApplication Closing Date: Sunday, 11 October 2026...Read More>>.

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Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates. Why IQVIA?...Read More>>.

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Act in the role of clinical site monitor to regularly visit/remotely assess in vitro diagnostic medical device clinical study sites and ensure that the study is conducted in compliance with the study protocol, ICH GCP and local regulatory requi...Read More>>.

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Parexel FSP is seeking an experienced Senior CRA to join a large Sponsor’s EU project. The role focuses on site management, monitoring and close-out of investigator sites to ensure patient safety and high-quality study execution.Key respo...Read More>>.

Parexel FSP is hiring for an experienced Senior CRA level to join one of our large Sponsor’s in the EU. Some specifics about this advertised role This role is responsible for the site management, site monitoring and close-out o...Read More>>.

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ICON Strategic Solutions, part of ICON, invites a Senior Clinical Research Associate to join sponsor-dedicated model, supported by ICON’s global expertise. As CRA II, you will design and analyse trials, interpret data, and contribute to developm...Read More>>.

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Thermo Fisher Scientific's PPD FSP division is seeking a Clinical Research Associate to support multinational clinical monitoring projects. You will perform on-site monitoring, ensure quality and compliance with ICH-GCP, EU and FDA requirements, a...Read More>>.

Thermo Fisher Scientific, through its PPD clinical research services, is seeking an experienced Assistant Clinical Research Associate (ACRA) to join our UK team. You will perform remote activities, support site management and monitoring processes,...Read More>>.

IQVIA is seeking a Senior Clinical Research Associate (cFSP sponsor-dedicated) in Reading to monitor sites and manage study data per protocol and GCP. You will coordinate monitoring visits, support recruitment plans, and ensure regulatory complian...Read More>>.

MSD is seeking a motivated Clinical Research Associate (CRA) to join our clinical operations team. The CRA serves as the primary site contact and site manager throughout all study phases, ensuring high-quality trial execution and compliance with I...Read More>>.

Our Clinical Operations (multi-sponsor) team in the UK is looking for a passionate CRA I with at least 6 months of independent monitoring experience to work across a diverse range of therapeutic areas – including Hematology/Oncology and Ophthalm...Read More>>.

Clinical Research AssociateDepartment: Corporate ServicesEmployment Type: Fixed Term - Full TimeLocation: RemoteCompensation: £28,560 / yearDescriptionPriory are looking to...Read More>>.

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